Abstract: An expandable tube for deployment within a blood vessel is disclosed. In one arrangement, the tube comprises an elongate frame that is reversibly switchable from a radially expanded and longitudinally contracted state to a radially contracted and longitudinally expanded state. The frame comprises a plurality of longitudinally deformable elements for providing longitudinal expansion and contraction of the frame and a plurality of circumferentially deformable elements for providing radial expansion and contraction of the frame. The longitudinally deformable elements can be expanded or contracted longitudinally substantially without any change in the shape of the circumferentially deformable elements. The plurality of circumferentially deformable elements comprises a plurality of sets of circumferentially deformable elements. Each set of circumferentially deformable elements forms a closed ring around an axis of elongation of the frame.

Abstract: Delivery systems for deploying a self-expanding tube into a blood vessel are disclosed. In one arrangement, a tubular member is provided that is configured for insertion into the blood vessel. An elongate body extends within a lumen of the tubular member. A self-expanding tube is positioned radially between the tubular member and the elongate body. Over at least 50% of the length of the self-expanding tube, at least a portion of the self-expanding tube engages outwardly with the tubular member and inwardly with the elongate body.

Abstract: A valve (100) for use in delivering a medical device comprises first and second ends and an hourglass shaped centre section defining an aperture (34) for accepting a guidewire. The application of torsion about the centre section closes the aperture to seal against the guidewire.

Abstract: A valve (100) for use in delivering a medical device comprises first and second ends and an hourglass shaped centre section defining an aperture (34) for accepting a guidewire. The application of torsion about the centre section closes the aperture to seal against the guidewire.

Abstract: A system (1) for delivering a staple (9) to the locus of an artery (2) comprises a delivery conduit (5) for inserting into the lumen of an artery through which conduit a staple can be delivered to the locus, and an elongate element (6) such as a catheter for a balloon (7) for translating axial advancement of the delivery conduit through the artery into movement of the distal end of the delivery conduit away from the longitudinal axis of the artery and towards the artery wall.

Abstract: A stent graft is provided which has two stent sections having different functions on, for example, a tubular graft. One stent section preferably comprises a plurality of circumferential reinforcing hoops and the other a Z-stent. The two sections are preferably separated by a spacer section and the tubular graft preferably increases in diameter from the Z-stent section to the hooped section. This enables the stent graft to be compressed radially so that it can be inserted in a catheter for later delivery to a body lumen.

Abstract: A stent graft can be held in place on the outside of the thoracic arch by a hypodermic needle tube which passes through a bore of the stent graft and back to the user. A center tube tethered to the stent graft at an end distal to the user is employed to hold the stent graft within the pulsatile blood flow, preventing the stent graft from collapsing during deployment. The position of both the hypodermic needle tube and the center tube can be controlled by the user by a control handle.

Abstract: Apparatus for deploying a tubular medical (200) device in vivo comprises an elongate element (10) for passing into the bore of the medical device, a deployment device having at least one arm for engaging with the medical device, the arm being moveable in a radial direction relative to the longitudinal axis of the elongate element from a first position to a second position, the second position being spaced radially further from the elongate element than the first position, and a thread (60) for the arm, said thread being associated with the arm such that pulling on the thread moves said arm from the second position towards the first position, whereby in use movement of the arm from the first position to the second position enables radial deployment of the medical device.

Abstract: A device is provided for piercing a graft and artery wall in order to retain the graft on the artery. The device has a central section with an abutment surface for contacting the inner wall of the graft and two elongate members with distal ends for contacting the outer wall of the artery when the device is pierced through the graft and artery. The elongate members are biased so as to urge the abutment surface into the graft and retain the graft on the artery.

Abstract: A stent graft can be held in place on the outside of the thoracic arch by a hypodermic needle tube which passes through the bore of the stent graft and back to the user. A centre tube tethered to the stent graft at the end distal to the user is employed to hold the stent graft within the pulsatile blood flow, preventing the stent graft from collapsing during deployment. The position of both the hypodermic needle tube and the centre tube can be controlled by the user by means of a control handle.

Abstract: In vivo failure of a helical stent graft is addressed by provision of reinforcing material for the graft material in at least two (preferably three) separate sections, each section comprising a continuous integral piece of material, wherein each section of reinforcing material is in the form of a helix with a longitudinal axis substantially parallel to the longitudinal axis of the tube. Thus leaks caused by unravelling of the reinforcing material are mitigated.

Abstract: A device is provided for piercing a graft and artery wall in order to retain the graft on the artery. The device has a central section with an abutment surface for contacting the inner wall of the graft and two elongate members with distal ends for contacting the outer wall of the artery when the device is pierced through the graft and artery. The elongate members are biased so as to urge the abutment surface into the graft and retain the graft on the artery.

Abstract: An articulated device for advancing a medical implant along a catheter comprises a plurality of segments (1, 12) arranged one after the other in line, each segment being hingeably connected to a single adjacent segment if it is at the end of the line and otherwise to two adjacent segments, whereby a medical implant mounted at one end of the device can be advanced through a catheter by pushing on the other end of the device, the hinged connections allowing the device to follow a curved path through the catheter.

Abstract: A device is provided for piercing a graft and artery wall in order to retain the graft on the artery. The device has a central section with an abutment surface for contacting the inner wall of the graft and two elongate members with distal ends for contacting the outer wall of the artery when the device is pierced through the graft and artery. The elongate members are biased so as to urge the abutment surface into the graft and retain the graft on the artery.

Abstract: A system (1) for delivering a staple (9) to the locus of an artery (2) comprises a delivery conduit (5) for inserting into the lumen of an artery through which conduit a staple can be delivered to the locus, and an elongate element (6) such as a catheter for a balloon (7) for translating axial advancement of the delivery conduit through the artery into movement of the distal end of the delivery conduit away from the longitudinal axis of the artery and towards the artery wall.

Abstract: A method for testing the pulsatile endurance of a vascular implant 3 comprises placing a resilient insert 4 into the implant and repeatedly expanding and contracting the insert, thereby expanding and contracting the implant. The insert preferably has a cavity therein and is repeatedly expanded and contracted by repeatedly increasing and decreasing the pressure in the cavity.

Abstract: A stent graft is provided which has two stent sections having different functions on, for example, a tubular graft. One stent section preferably comprises a plurality of circumferential reinforcing hoops and the other a Z-stent. The two sections are preferably separated by a spacer section and the tubular graft preferably increases in diameter from the Z-stent section to the hooped section. This enables the stent graft to be compressed radially so that it can be inserted in a catheter for later delivery to a body lumen.

Abstract: A control mechanism comprises an elongate handle 10 having an external thread 12 and a barrel 20 with internally projecting pins 21 threaded over handle 10. Rotation of barrel 20 causes handle 10 to move back and forth along its longitudinal axis to retract and advance a catheter sheath to which handle 10 is coupled, thereby enabling an implant to be deployed by the catheter. Rotation movement of barrel 20 and longitudinal movement of handle 10 can be disassociated to enable speedy retraction or advancement of the catheter sheath.

Abstract: A device is provided for piercing a graft and artery wall in order to retain the graft on the artery. The device has a central section with an abutment surface for contacting the inner wall of the graft and two elongate members with distal ends for contacting the outer wall of the artery when the device is pierced through the graft and artery. The elongate members are biased so as to urge the abutment surface into the graft and retain the graft on the artery.